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Clinical Trial Summary

The purpose of this trial was to demonstrate the efficacy and safety of everolimus in combination with reduced tacrolimus, compared to tacrolimus control, in living donor liver transplant recipients.


Clinical Trial Description

This study was 24 month, multicenter study in 280 living donor liver transplant patients from Asia, Europe and Canada. The study has an long term extension in Japan and approximately 28 patients were to be included to evaluate the long-term efficacy and safety of concentration-controlled everolimus regimen plus reduced tacrolimus compared to standard tacrolimus in recipients of living donor liver transplants in Japan who participated in the CRAD001H2307 study.

Data reported here are the CRAD001H2307 core study results and its extension (CRAD001H2307E1). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01888432
Study type Interventional
Source Novartis
Contact
Status Completed
Phase Phase 3
Start date September 25, 2013
Completion date April 21, 2018

See also
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